Antioxidant 1,2,3,4,6-Penta-O-galloyl-β-D-glucose Alleviating Apoptosis and Promoting Bone Formation Is Associated with Estrogen Receptors

被引:0
|
作者
Hua, Yongqing [1 ,2 ,3 ]
Wang, Haili [2 ]
Chen, Tingting [2 ]
Zhou, Yeru [4 ]
Chen, Zhiyuan [2 ]
Zhao, Xinyue [2 ]
Mo, Shaoqin [2 ]
Mao, Hongyun [2 ]
Li, Miao [2 ]
Wang, Linxia [2 ]
Hong, Min [1 ,2 ,3 ]
机构
[1] Nanjing Univ Chinese Med, Jiangsu Collaborat Innovat Ctr Chinese Med Resourc, Natl & Local Collaborat Engn Ctr Chinese Med Resou, Nanjing 210023, Peoples R China
[2] Nanjing Univ Chinese Med, Sch Pharm, Nanjing 210023, Peoples R China
[3] Nanjing Univ Chinese Med, Jiangsu Key Lab Pharmacol & Safety Evaluat Chinese, Nanjing 210023, Peoples R China
[4] Nanjing Univ Chinese Med, Sch Med & Holist Integrat Med, Nanjing 210023, Peoples R China
来源
MOLECULES | 2024年 / 29卷 / 21期
基金
中国国家自然科学基金;
关键词
osteoporosis; zebrafish; estrogen receptor alpha; nuclear factor erythroid 2-related factor 2; reactive oxygen species; PAEONIA-LACTIFLORA; OXIDATIVE STRESS; CANCER CELLS; PENTAGALLOYLGLUCOSE; ACTIVATION; PATHWAY; ALPHA; NRF2;
D O I
10.3390/molecules29215110
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
1,2,3,4,6-penta-O-galloyl-beta-D-glucose (PGG) is the main phenolic active ingredient in Paeoniae Radix Alba, which is commonly used for the treatment of osteoporosis (OP). PGG is a potent natural antioxidant, and its effects on OP remain unknown. This study aimed to investigate the effects of PGG on promoting bone formation and explore its estrogen receptor (ER)-related mechanisms. A hydrogen peroxide-induced osteoblast apoptosis model was established in MC3T3-E1 cells. The effects of PGG were assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, flow cytometry, alkaline phosphatase (ALP) staining, RT-qPCR, and Western blot methods. Furthermore, a prednisolone-induced zebrafish OP model was employed to study the effects in vivo. ER inhibitors and molecular docking methods were used further to investigate the interactions between PGG and ERs. The results showed that PGG significantly enhanced cell viability and decreased cell apoptosis by restoring mitochondrial function, attenuating reactive oxygen species levels, decreasing the mitochondrial membrane potential, and enhancing ATP production. PGG enhanced ALP expression and activity and elevated osteogenic differentiation. PGG also promoted bone formation in the zebrafish model, and these effects were reversed by ICI182780. These results provide evidence that the effects of PGG in alleviating apoptosis and promoting bone formation may depend on ERs. As such, PGG is considered a valuable candidate for treating OP.
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页数:25
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